HEREDITARY glycinuria.
[No authors listed]
Nutr Rev. 1958 Feb;16(2):48-50. doi: 10.1111/j.1753-4887.1958.tb00667.x.
Glycinuria.
WOOLF LI.
Bull Schweiz Akad Med Wiss. 1962 Jan;17:382-4.
CALCIUM AND GLYCINURIA IN OSTEOMALACIA.
DUBOVSKY J.
Lancet. 1965 Mar 13;1(7385):602. doi: 10.1016/s0140-6736(65)91181-5.
Glycinuria, a hereditary disorder associated with nephrolithiasis.
DE VRIES A, KOCHWA S, LAZEBNIK J, FRANK M, DJALDETTI M.
Am J Med. 1957 Sep;23(3):408-15. doi: 10.1016/0002-9343(57)90320-0.
[Renal glycinuria and aminoaciduria associated with oligophrenia. Clinical and biochemical study].
Mardens Y, Adriaenssens K, Van Sande M.
J Neurol Sci. 1968 Mar-Apr;6(2):333-46. doi: 10.1016/0022-510x(68)90100-7.
Hyperglycinuria: diagnosis in middle age.
Fargaly H, Mathew S, Rossi NF.
BMJ Case Rep. 2022 Mar 2;15(3):e246252. doi: 10.1136/bcr-2021-246252.
Glycinuria following administration of glycine-supplemented oral rehydration solution in rotavirus diarrhoea.
Vesikari T, Isolauri E, Marnela KM.
Acta Paediatr Scand. 1988 Jan;77(1):165-6. doi: 10.1111/j.1651-2227.1988.tb10619.x.
A combined defect of three mitochondrial carboxylases presenting as biotin-responsive 3-methylcrotonyl glycinuria and 3-hydroxyisovaleric aciduria.
Bartlett K, Ng H, Leonard JV.
Clin Chim Acta. 1980 Jan 15;100(2):183-6. doi: 10.1016/0009-8981(80)90081-9.
[Gluco-glycinuria, a new familial syndrome].
KAESER H, COTTIER P, ANTENER I.
Helv Paediatr Acta. 1961 Dec;16:586-608.
[Familial encephalopathy, imino-glycinuria, hydroxyprolinemia].
Ghisolfi J, Augier D, Fabre J, Delsol G, Régnier C.
Arch Fr Pediatr. 1972 Apr;29(4):336-7.
